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1 one precursor genes encoded by a filamentous ascomycete.
2 osporum, the other sequenced ectomycorrhizal ascomycete.
3 e, unmutated copy in the genomes of 11 other ascomycetes.
4 ared with those of 13 more distantly related Ascomycetes.
5 equence homologue of securins found in model ascomycetes.
6  fungal virulence factor in plant pathogenic ascomycetes.
7 imilar to those encoded by other filamentous ascomycetes.
8 er in specificity at het loci in filamentous ascomycetes.
9 the control of sexual differentiation in the ascomycetes.
10 ed virulence determinant of plant pathogenic ascomycetes.
11 ly during sexual reproduction in filamentous ascomycetes.
12 regulates sexual reproduction in filamentous ascomycetes.
13 genes as observed in homothallic filamentous Ascomycetes.
14 s and humans but surprisingly absent in most ascomycetes.
15  are found predominantly in lignin-degrading ascomycetes.
16 ing Ophiocordyceps species, and not in other ascomycetes.
17  which might act as antifungal drugs against ascomycetes.
18 also provide insight into early evolution of ascomycetes.
19 ntaining and generating the diversity of the ascomycetes.
20 s, some of which are also conserved in other ascomycetes.
21 exin that is conserved across diverse fungal ascomycetes.
22 s large and diverse family of lichen-forming ascomycetes.
23 es and beta2-tubulin genes were lost in most ascomycetes.
24 tion of Nbp2p appears to be conserved across Ascomycetes.
25 ication is required for successful mating in ascomycetes.
26 .181) versus 1.210 (95% CI, 1.161-1.261) for ascomycetes, 1.112 (95% CI, 1.085-1.14) versus 1.302 (95
27 d that homologs of DES are widespread in the ascomycetes, although in most cases the homologs must pa
28 eptor and pheromone genes from a filamentous ascomycete and a basidiomycete and expressed these in th
29 scovered that Nbp2p orthologues exist in all Ascomycete and Basidiomycete fungal genomes and that all
30 fy over 50 putative pathways in a variety of ascomycete and basidiomycete fungi and functionally vali
31                                          The ascomycete and basidiomycete fungi have contributed much
32 ters used in these vectors function in other ascomycete and basidiomycete fungi, we anticipate that t
33 or of angiosperm plants but is ubiquitous in ascomycete and basidiomycete fungi.
34 ranscription in non-symbiotic fungi from the Ascomycete and Basidiomycete phyla.
35 o significantly inversely correlated with EM Ascomycete and EM short-contact exploration type abundan
36 hat are a major constituent of cell walls in Ascomycetes and Basidiomycetes fungi.
37 resses two Galpha subunits, most filamentous ascomycetes and basidiomycetes have three Galpha subunit
38 onophyletic clade of fungi, the Dikarya (the ascomycetes and basidiomycetes), and the ancestral state
39 repressor Ssd1, which is highly conserved in ascomycetes and basidiomycetes.
40 NA editing during sexual reproduction in two ascomycetes and deletion of FgATG11, the ATG gene with t
41         Notably, warming strongly favored EM Ascomycetes and EM fungi with short-contact hyphal explo
42 olves the relationships of numerous "orphan" ascomycetes and establishes the independent evolutionary
43 lls for mating are found only in filamentous ascomycetes and even here, a single individual produces
44 Transcription factor Rme1 is conserved among ascomycetes and regulates meiosis and pseudohyphal growt
45        The higher fungi are divided into the ascomycetes and the basidiomycetes.
46 alcineurin-responsive zinc fingers (Crz1) of ascomycetes and to the Pkc1-dependent specificity protei
47 ymbiosis between a single fungus, usually an ascomycete, and a photosynthesizing partner.
48 diomycete to be successfully expressed in an ascomycete, and paves the way for the exploitation of a
49 linked genomics-metabolomics dataset for 110 Ascomycetes, and optimized both gene cluster family (GCF
50                                          The ascomycete Brewer's yeast (Saccharomyces cerevisiae) was
51 in controlling asexual growth in filamentous Ascomycetes but also confirm that heterothallic and homo
52 ate that the separase homologue Esp1p in the ascomycete Candida albicans, an important pathogen of hu
53 ex, long treated as a zone of differentiated ascomycete cells, appears to consistently contain two un
54 ere, we analysed 16 European isolates of the ascomycete Cenococcum geophilum, an extremely ubiquitous
55 ly encountered symbiont on tree roots is the ascomycete Cenococcum geophilum, the only mycorrhizal sp
56 invasive human mycoses caused by the phaeoid ascomycete, Chaetomium perlucidum, and review the Englis
57 reviously isolated from a vorinostat-treated ascomycete Chalara sp., was prepared in nine steps from
58                                 The haploid, ascomycete chestnut blight pathogen, Cryphonectria paras
59         (+)-Chloriolide, a metabolite of the ascomycete Chloridium virescens var. chlamydosporum, was
60 aria inaequalis, a widely distributed litter ascomycete, chlorinated the aromatic rings of lignin in
61             FlbC is conserved in filamentous Ascomycetes containing two C(2) H(2) zinc fingers at the
62  entrapped cellobiose dehydrogenase from the ascomycete Corynascus thermophilus (CtCDH) in a photocro
63 of chestnut blight caused by the filamentous ascomycete Cryphonectria parasitica can be achieved with
64                                          The ascomycete Cryphonectria parasitica causes destructive c
65 in the tripartite pathosystem.IMPORTANCE The ascomycete Cryphonectria parasitica causes destructive c
66 diversification; in the clade of filamentous ascomycetes, dense-core Woronin bodies bud from peroxiso
67 itis are dimorphic, soil-dwelling pathogenic ascomycetes endemic to the southwestern United States.
68 ated with resistance to the broad host range ascomycete entomopathogen Metarhizium anisopliae (Ma549)
69 hogen effectors from three branches of life (ascomycete, eubacteria, and oomycete) converge onto the
70 MAT/MTL) has controlled cell type throughout ascomycete evolution.
71                                      Several ascomycetes explain lowered yield as soybean pathogens i
72 esent classification, be placed in different ascomycete families: the Microcyclus sexual morph in the
73 nary history of spore shapes within a single ascomycete family we measure the relative contributions
74 nd electron microscopy to show that a common Ascomycete filamentous fungus, Stilbella aciculosa, oxid
75  sp. hordei (Bgh), is an obligate biotrophic ascomycete fungal pathogen that can grow and reproduce o
76 A polymerase III (Pol III), while animal and ascomycete fungal TERs are transcribed by RNA Pol II and
77 thylguanosine (TMG) cap common to animal and ascomycete fungal TERs.
78         Anthracnose disease is caused by the ascomycetes fungal species Colletotrichum, which is resp
79  not previously known for mosses, as well as ascomycete fungi (e.g. Rhizoscyphus ericae) that associa
80 ion is not required for successful mating of ascomycete fungi and confirm that, in budding yeast, the
81 d S. japonicus--occupies the basal branch of Ascomycete fungi and is an important model of eukaryote
82 th is a ubiquitous phenomenon in filamentous ascomycete fungi and is termed heterokaryon incompatibil
83 a distinct group that was closely related to ascomycete fungi and that human-derived P. carinii was m
84 oscopic size, the forcibly ejected spores of ascomycete fungi are quickly brought to rest by drag.
85 ve the signature of horizontal transfer from ascomycete fungi associated with wood decay and from pro
86 conserved in the genomes of most filamentous ascomycete fungi capable of degrading cellulose.
87 dly permeabilizes the plasma membrane of the ascomycete fungi Fusarium graminearum and Neurospora cra
88              The forcibly launched spores of ascomycete fungi must eject through several millimeters
89                    During sexual development ascomycete fungi produce two types of peptide pheromones
90  a defensin which inhibits the growth of two ascomycete fungi via different mechanisms.
91 termediate- and late-stage soils, lichenized ascomycete fungi were prevalent, but bacteria increasing
92 elic mating-type locus (e.g., Chlamydomonas, ascomycete fungi).
93 s spp. examined, in several other classes of ascomycete fungi, and in animals but not in basidiomycet
94 l glycine-leucine motif in SREBP homologs of ascomycete fungi, including the opportunistic human path
95 llus flavus, like approximately one-third of ascomycete fungi, is thought to be cosmopolitan and clon
96 ant defensin, MtDef4, inhibits growth of the ascomycete fungi, Neurospora crassa and Fusarium gramine
97               Using two common environmental Ascomycete fungi, Paraconiothyrium sporulosum and Stagon
98                          Instead, a range of ascomycete fungi, termed dark septate endophytes (DSEs),
99 ions of four species of facultatively sexual ascomycete fungi, which have been jointly scored for mat
100 female and male behaviour in the filamentous ascomycete fungi.
101 ll other eukaryotes except a small number of ascomycete fungi.
102 of ensuing Mn oxides by six Mn(II)-oxidizing Ascomycete fungi.
103 1, a regulator of cell-type specification in ascomycete fungi.
104                                       In the Ascomycete fungus Aspergillus nidulans, the ratio of con
105 ic interactions with natural variants of the ascomycete fungus Blumeria graminis f. sp. hordei (Bgh),
106 ic interactions with natural variants of the ascomycete fungus Blumeria graminis f.sp. hordei (Bgh),
107                           For the biotrophic ascomycete fungus Blumeria hordei (Bh) it has been shown
108                                          The ascomycete fungus Cercospora zeae-maydis is an aggressiv
109                                          The ascomycete fungus Cochliobolus carbonum race 1 is pathog
110                  Fusarium wilt caused by the ascomycete fungus Fusarium oxysporum is a devastating di
111                                          The ascomycete fungus Mycosphaerella graminicola is the caus
112 hain mutations using a genetic screen of the ascomycete fungus Neurospora crassa, in which dynein is
113 ng patterns of nuclear movement in the model ascomycete fungus Neurospora crassa, we show that geneti
114 ptional regulation of ribosomal genes in the ascomycete fungus Neurospora crassa.
115 he versatile lipase/sterol esterase from the ascomycete fungus O. piceae.
116                                          The ascomycete fungus Ophidiomyces ophiodiicola (Oo) is the
117 roach in a study of Coccidioides immitis, an ascomycete fungus responsible for a recent epidemic of c
118 letotrichum higginsianum is a hemibiotrophic ascomycete fungus that is adapted to Arabidopsis (Arabid
119  genome alignment of five individuals of the ascomycete fungus Zymoseptoria pseudotritici, a close re
120 ur study of the mating system of the haploid ascomycete fungus, Cryphonectria parasitica, resulted in
121  New cosmid vectors were constructed for the ascomycete fungus, Magnaporthe grisea and the basidiomyc
122 he isolation of a common mosquito-associated ascomycete fungus, Penicillium chrysogenum, from the mid
123 ic alpha-pheromone from the plant pathogenic ascomycete Fusarium oxysporum revealed the presence of a
124 ther with 451 genomes covering all available ascomycete genera.
125 ied a comparative genomic approach across 14 Ascomycete genomes, mapping phenotypes and genotypes ont
126 were unclassified and tended to be unique to ascomycete genomes.
127 ning HET domains are frequent in filamentous ascomycete genomes.
128 known to form meiotic (sexual) stages in the ascomycete genus Ajellomyces (Onygenaceae, Onygenales),
129 ith water treatment and were dominated by an ascomycete, Geopora sp.
130                                              Ascomycetes have just two mating types, but basidiomycet
131                                         Most ascomycetes have two mating types: one (called alpha in
132 s of other basidiomycete natural products in ascomycete heterologous hosts, and open up new possibili
133 y system, typical of other self-incompatible Ascomycetes, in which mating is only successful between
134 f its exclusive presence in the CTG clade of ascomycetes, including Candida albicans, a human pathoge
135                     Infection with divergent ascomycetes, including dimorphic fungi, opportunistic mo
136  mainly in the coding regions in filamentous ascomycetes, involving adenosine deamination mechanisms
137 n of this well-conserved gene in filamentous ascomycetes is not clear.
138 olution of the biologically diverse forms of ascomycetes is not well understood, largely because the
139  (phylum Ascomycota) but not early diverging ascomycetes, like Saccharomyces cerevisiae (Saccharomyco
140 e last common ancestor of basidiomycetes and ascomycetes likely possessed two paralogs of alpha-tubul
141 ese substrates with orthologs throughout the ascomycete lineage revealed that the position of most ph
142     Peroxidases of unknown function from the ascomycete Magnaporthe grisea were found to be the close
143                                         Most ascomycete mating-type loci are structurally complex idi
144  of H3K9me2/3 heterochromatin, the origin of ascomycete mating-type switching, and panascomycete synt
145                               In most fungal ascomycetes, mating is controlled by a single locus (MAT
146 s, among them sexuality.(1) In heterothallic ascomycetes, mating-type systems ensure that only compat
147 zation is also predicted to be common in the ascomycete mould, Neurospora crassa.
148               Like its homologues from other ascomycetes, Mst7 contains a putative MAPK-docking site
149   Deletion of the homolog in the filamentous ascomycete Neurospora crassa affects the circadian clock
150 gi--or fungi in general other than the model ascomycete Neurospora crassa--has been neglected, leavin
151 encoded by the anx14 gene of the filamentous ascomycete Neurospora crassa.
152 ape of spore killing, and in the filamentous ascomycete Neurospora sitophila, the Sk-1 spore killer e
153          Vegetative cells of the filamentous ascomycete Neurospora tetrasperma are typically heteroka
154 quality genomic data sets of the filamentous ascomycete Neurospora tetrasperma, a fungus that lacks r
155 own alga Ectocarpus sp. (Chromista), and the ascomycetes Neurospora crassa and Aspergillus nidulans (
156 type has been reported in several species of Ascomycetes, no peptide has been reported to function as
157 e family provides a compelling example in an ascomycete of chromatin-based silencing of natural subte
158      We report the identification of a novel Ascomycete PAMP, RcCDI1, recognized by Solanaceae but no
159 tion network of virulence effectors from the ascomycete pathogen Golovinomyces orontii and Arabidopsi
160 ation pattern and symptom development by the ascomycete pathogen Plectosphaerella cucumerina (P. cucu
161                                           In ascomycetes, perithecium development involves sexual dif
162                   Pneumocystis carinii is an ascomycete phylogenetically related to Schizosaccharomyc
163    Sclerotinia sclerotiorum is a filamentous ascomycete phytopathogen able to infect an extremely wid
164 ating functional conservation in filamentous ascomycete phytopathogens and saprobes.
165 basidiomycete Ustilago maydis (UmAbf62A) and ascomycete Podospora anserina (PaAbf62A).
166 ndo-beta-1,4-mannanases from the coprophilic ascomycete Podospora anserina contribute to the enzymati
167                                        While ascomycetes predominantly have a bipolar mating system w
168  Neurospora crassa and related heterothallic ascomycetes produce eight homokaryotic self-sterile asco
169                                          The ascomycete Saccharomyces cerevisiae exhibits alternative
170 is more reminiscent of the distantly related ascomycete, Schizosaccharomyces pombe.
171 studies have begun to reveal how filamentous ascomycete species exploit carbon sources in different h
172 nzymatically cycling recalcitrant carbon, to Ascomycete species that have melanized cell walls that a
173 ovel genes in N.crassa and other filamentous ascomycete species.
174 se in functional coordination with versatile Ascomycete species.
175                 Therefore, pseudohomothallic ascomycetes such as N. tetrasperma face an apparent evol
176                                           In ascomycetes such as Saccharomyces cerevisiae and Candida
177 ly to be complemented well by EF3 from other ascomycetes, such as Candida albicans.
178     Genomic and phylogenetic analyses across ascomycetes suggest that the Spok genes disperse through
179                  The conservation of cpsA in Ascomycetes suggests that cpsA homologs might have simil
180 e slow-growing environmental rock-inhabiting ascomycete synthesizing a constitutive DHN-melanin, Cryo
181  gene family 11 (GH11) was obtained from the ascomycete Talaromyces amestolkiae.
182 slow-growing spruces had a greater number of Ascomycete taxa and free-living saprotrophic fungi.
183                                   While most Ascomycetes tend to associate principally with plants, t
184 t infects the fungus Rosellinia necatrix, an ascomycete that is pathogenic to a wide range of plants.
185 s evidently belongs to an extinct lineage of ascomycetes that could serve as a minimum node age calib
186 plete loss of annexin sequences from another ascomycete, the budding yeast Saccharomyces cerevisiae.
187 any common lichens are composed of the known ascomycete, the photosynthesizing partner, and, unexpect
188                                 Thus, in the ascomycetes, the Ifh1-Fhl1 heterodimer has reconfigured
189                                           In ascomycetes, the single mating type locus (MAT) controls
190 f MAT genes from a wide array of filamentous ascomycetes, thereby providing MAT-based technology for
191 transceptor activity likely occur in related ascomycetes used for industrial cellulase production.
192 graphic history of worldwide invasion of the ascomycete Verticillium dahliae, a soil-borne pathogen,
193 le the relative percent of tips colonized by Ascomycetes was positively correlated with soil pH.
194                                    Ancestral ascomycetes were filamentous; hyphal growth was lost ind
195 ilable for alpha pheromones from filamentous ascomycetes, which are significantly shorter and share a
196 ungi are less tractable genetically than the ascomycetes, which predominantly produce lower-potential
197 zae giving production of pleuromutilin in an ascomycete, with a significant increase (2106%) in produ
198 viously uncharacterized proteins specific to Ascomycetes, with SAD-4 having a range that spans severa
199 cription regulatory hubs in recent course of ascomycete yeast evolution.
200 r a reticulon-like protein in species of the ascomycete yeast genus Lipomyces, the most 5' terminal i
201         This circuit regulates mating in the ascomycete yeast lineage.
202 hich is known to be involved in autophagy in ascomycete yeast, was defective in the formation of auto
203 rates an evolutionary divergence from EF3 of ascomycete yeast.
204  However, EF3 has been characterized only in ascomycete yeast.
205                                              Ascomycete yeasts are metabolically diverse, with great
206 pproximately 200 million y ago in a clade of ascomycete yeasts that includes Saccharomyces cerevisiae
207 such as the early diverging lineages and the ascomycete yeasts, but was otherwise slightly inferior t
208 red through a series of experiments in three ascomycete yeasts: the bakers' yeast Saccharomyces cerev

 
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